ATE293102T1 - NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE - Google Patents
NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USEInfo
- Publication number
- ATE293102T1 ATE293102T1 AT99917102T AT99917102T ATE293102T1 AT E293102 T1 ATE293102 T1 AT E293102T1 AT 99917102 T AT99917102 T AT 99917102T AT 99917102 T AT99917102 T AT 99917102T AT E293102 T1 ATE293102 T1 AT E293102T1
- Authority
- AT
- Austria
- Prior art keywords
- sup
- substituted
- group
- hydrogen atom
- sub
- Prior art date
Links
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical class C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 title 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 201000011510 cancer Diseases 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 241000124008 Mammalia Species 0.000 abstract 1
- 206010027476 Metastases Diseases 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000009401 metastasis Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- IHOBBYHEOBWAPZ-UHFFFAOYSA-L steroid c Chemical compound [Na+].[Na+].C1CC2CC(OS([O-])(=O)=O)C(OS([O-])(=O)=O)CC2(C)C(CCC23C)C1C3CC(O1)C2C2(C)OC1OC2CC(C(C)C)=C(C)C IHOBBYHEOBWAPZ-UHFFFAOYSA-L 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Fats And Perfumes (AREA)
Abstract
A composition containing a compound of the formula: wherein A is a nitrogen-containing heterocyclic group which may be substituted, R<SUP>1 </SUP>is a hydrogen atom, hydrocarbon group which may be substituted, or monocyclic aromatic heterocyclic group which may be substituted, R<SUP>2 </SUP>is a hydrogen atom or a lower alkyl group which may be substituted, R<SUP>3</SUP>, R<SUP>4</SUP>, R<SUP>5</SUP>, R<SUP>6</SUP>, R<SUP>7</SUP>, R<SUP>8 </SUP>and R<SUP>9 </SUP>are independently a hydrogen atom, a hydrocarbon group which may be substituted, a hydroxy group which may be substituted, a thiol group which may be substituted, an amino group which may be substituted, an acyl group or a halogen atom, a salt thereof or a prodrug thereof has steroid C<SUB>17,20</SUB>-lyase inhibitory activity, and are useful for preventing and treating a mammal suffering from, for example, primary cancer of malignant tumor, its metastasis and recurrence thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11380198 | 1998-04-23 | ||
| PCT/JP1999/002143 WO1999054309A1 (en) | 1998-04-23 | 1999-04-22 | Naphthalene derivatives, their production and use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE293102T1 true ATE293102T1 (en) | 2005-04-15 |
Family
ID=14621427
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT99917102T ATE293102T1 (en) | 1998-04-23 | 1999-04-22 | NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US6573289B1 (en) |
| EP (1) | EP1073640B1 (en) |
| AT (1) | ATE293102T1 (en) |
| AU (1) | AU3534699A (en) |
| CA (1) | CA2328973A1 (en) |
| DE (1) | DE69924717T2 (en) |
| WO (1) | WO1999054309A1 (en) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070129282A1 (en) * | 1998-11-24 | 2007-06-07 | Ahlem Clarence N | Pharmaceutical treatments and compositions |
| DE60045474D1 (en) | 1999-01-13 | 2011-02-17 | Univ New York State Res Found | NEW METHOD FOR CREATING PROTEIN KINASE INHIBITORS |
| WO2000078727A1 (en) * | 1999-06-22 | 2000-12-28 | Takeda Chemical Industries, Ltd. | Process for the preparation of imidazole derivatives |
| CA2669753C (en) * | 1999-09-30 | 2012-06-26 | Hollis-Eden Pharmaceuticals, Inc. | Therapeutic treatment of androgen receptor driven conditions |
| AU7950100A (en) * | 1999-10-22 | 2001-05-08 | Takeda Chemical Industries Ltd. | 1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof |
| PE20010781A1 (en) * | 1999-10-22 | 2001-08-08 | Takeda Chemical Industries Ltd | COMPOUNDS 1- (1H-IMIDAZOL-4-IL) -1- (NAFTIL-2-SUBSTITUTED) ETHANOL, ITS PRODUCTION AND USE |
| DE60026725T2 (en) * | 1999-10-22 | 2006-09-07 | Takeda Pharmaceutical Co. Ltd. | METHOD FOR THE PRODUCTION OF OPTICALLY ACTIVE NAPHTHALINE DERIVATIVES AND OPTICAL RESOLVERS THEREOF |
| JP3753971B2 (en) | 2000-11-17 | 2006-03-08 | 武田薬品工業株式会社 | Novel imidazole derivatives, their production and use |
| DE60144246D1 (en) | 2000-11-20 | 2011-04-28 | Takeda Pharmaceutical | IMIDAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE |
| AU2002221080A1 (en) | 2000-12-08 | 2002-06-18 | Masami Kusaka | Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparingthe same and use thereof |
| WO2003015820A1 (en) * | 2001-08-10 | 2003-02-27 | Takeda Chemical Industries, Ltd. | GnRH AGONIST COMBINATION DRUGS |
| CA2464214C (en) * | 2001-10-22 | 2011-02-08 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors, methods for designing them, and methods of using them |
| US7005445B2 (en) | 2001-10-22 | 2006-02-28 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors and methods for designing them |
| EP1654236A1 (en) * | 2003-07-10 | 2006-05-10 | OSI Pharmaceuticals, Inc. | Naphthylene derivatives as cytochrome p450 inhibitors |
| WO2005073224A2 (en) | 2004-01-23 | 2005-08-11 | Amgen Inc | Quinoline quinazoline pyridine and pyrimidine counds and their use in the treatment of inflammation angiogenesis and cancer |
| WO2005070891A2 (en) | 2004-01-23 | 2005-08-04 | Amgen Inc | Compounds and methods of use |
| US7662844B2 (en) | 2004-07-12 | 2010-02-16 | Osi Pharmaceuticals, Inc. | Naphthylene derivatives as cytochrome P450 inhibitors |
| JP2008521900A (en) | 2004-11-30 | 2008-06-26 | アムジエン・インコーポレーテツド | Quinolines and quinazoline analogues and their use as medicaments for the treatment of cancer |
| JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Substituted Amid derivatives & methods of use |
| CN101374832B (en) * | 2006-01-27 | 2013-03-06 | 弗·哈夫曼-拉罗切有限公司 | Use of 4-imidazole derivatives for CNS disorders |
| US7838542B2 (en) | 2006-06-29 | 2010-11-23 | Kinex Pharmaceuticals, Llc | Bicyclic compositions and methods for modulating a kinase cascade |
| WO2008046756A1 (en) * | 2006-10-19 | 2008-04-24 | F. Hoffmann-La Roche Ag | Aminomethyl-2-imidazoles with affinity with the trace amine associated receptors |
| CA2666762C (en) * | 2006-10-19 | 2014-12-30 | F. Hoffmann-La Roche Ag | Aminomethyl-4-imidazoles |
| EP2086959B1 (en) | 2006-11-02 | 2011-11-16 | F. Hoffmann-La Roche AG | Substituted 2-imidazoles as modulators of the trace amine associated receptors |
| MX2009005047A (en) * | 2006-11-16 | 2009-05-25 | Hoffmann La Roche | Substituted 4-imidazoles. |
| MX2009005920A (en) * | 2006-12-13 | 2009-06-16 | Hoffmann La Roche | Novel 2 -imidazoles as ligands for trace amine associated receptors (taar). |
| US20080146523A1 (en) * | 2006-12-18 | 2008-06-19 | Guido Galley | Imidazole derivatives |
| MX2009008255A (en) * | 2007-02-02 | 2009-08-12 | Hoffmann La Roche | Novel 2-aminooxazolines as taar1 ligands for cns disorders. |
| KR101222412B1 (en) * | 2007-02-15 | 2013-01-15 | 에프. 호프만-라 로슈 아게 | 2-aminooxazolines as taar1 ligands |
| CN101687812A (en) | 2007-07-02 | 2010-03-31 | 弗·哈夫曼-拉罗切有限公司 | 2-Imidazoline Compounds with Good Affinity for Trace Amine-Associated Receptors (TAARs) |
| WO2009003867A1 (en) * | 2007-07-03 | 2009-01-08 | F. Hoffmann-La Roche Ag | 4-imidazolines and their use as antidepressants |
| WO2009016048A1 (en) * | 2007-07-27 | 2009-02-05 | F. Hoffmann-La Roche Ag | 2-azetidinemethaneamines and 2-pyrrolidinemethaneamines as taar-ligands |
| CN101765425A (en) * | 2007-08-02 | 2010-06-30 | 弗·哈夫曼-拉罗切有限公司 | Use of benzamide derivatives for the treatment of CNS disorders |
| BRPI0814758A2 (en) * | 2007-08-03 | 2015-03-03 | Hoffmann La Roche | PYRIDINACARBOXAMIDE AND BENZAMIDE DERIVATIVES AS TAAR BINDERS |
| MX2010004620A (en) * | 2007-10-29 | 2010-07-28 | Amgen Inc | Benzomorpholine derivatives and methods of use. |
| US8242153B2 (en) * | 2008-07-24 | 2012-08-14 | Hoffmann-La Roche Inc. | 4,5-dihydro-oxazol-2YL derivatives |
| CN102083805A (en) * | 2008-07-24 | 2011-06-01 | 弗·哈夫曼-拉罗切有限公司 | 4, 5-dihydro-oxazol-2-yl derivs |
| US20100311798A1 (en) * | 2009-06-05 | 2010-12-09 | Decoret Guillaume | 2-aminooxazolines as taar1 ligands |
| UY32730A (en) | 2009-06-26 | 2011-01-31 | Novartis Ag | CYP17 INHIBITORS |
| US8354441B2 (en) * | 2009-11-11 | 2013-01-15 | Hoffmann-La Roche Inc. | Oxazoline derivatives |
| US9452980B2 (en) | 2009-12-22 | 2016-09-27 | Hoffmann-La Roche Inc. | Substituted benzamides |
| JP6106437B2 (en) | 2010-01-07 | 2017-03-29 | アルカーメス ファーマ アイルランド リミテッド | Prodrugs of heteroaromatic compounds |
| KR101926320B1 (en) | 2010-08-04 | 2018-12-06 | 펠피큐어 파마슈티걸즈 아이엔씨 | Combination therapy for the treatment of prostate carcinoma |
| EP2627648A1 (en) | 2010-09-16 | 2013-08-21 | Novartis AG | 17aHYDROXYLASE/C17,20-LYASE INHIBITORS |
| AU2011326487B2 (en) * | 2010-11-13 | 2017-03-02 | Innocrin Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
| MX359399B (en) | 2011-04-28 | 2018-09-27 | Novartis Ag | 17a-HYDROXYLASE/C17,20-LYASE INHIBITORS. |
| JP2014525442A (en) * | 2011-08-30 | 2014-09-29 | ヴィアメット ファーマスーティカルズ,インコーポレイテッド | Metalloenzyme inhibitory compounds |
| WO2014158875A1 (en) | 2013-03-14 | 2014-10-02 | Pellficure Pharmaceuticals Inc. | Novel therapy for prostate carcinoma |
| CA2960750A1 (en) | 2014-09-12 | 2016-03-17 | Pellficure Pharmaceuticals, Inc. | Compositions and methods for treatment of prostate carcinoma |
| JP6814814B2 (en) | 2016-03-17 | 2021-01-20 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 5-Ethyl-4-methyl-pyrazole-3-carboxamide derivative with activity as an agonist of TAAR |
| WO2018080933A1 (en) | 2016-10-24 | 2018-05-03 | Pellficure Pharmaceuticals Inc. | Pharmaceutical compositions of 5-hydroxy-2-methylnaphthalene-1, 4-dione |
| CN114213296B (en) * | 2021-12-23 | 2024-01-26 | 中节能万润股份有限公司 | Naphthalene series liquid crystal monomer compound containing isothiocyanato and preparation method and application thereof |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1154722A (en) * | 1965-07-08 | 1969-06-11 | Boots Pure Drug Co Ltd | 2,4,5-Tribromoimidazole Derivatives and Compositions thereof |
| US3759934A (en) * | 1970-12-09 | 1973-09-18 | Sandoz Ag | 2,3 or 4-pyri dinemethanol-alpha-substituted or unsubstituted phenyls-alpha-(2 or 3-alkoxy-1-naphthyls) |
| DE3373467D1 (en) | 1982-06-14 | 1987-10-15 | Takeda Chemical Industries Ltd | Vinyl carboxylic acid derivatives, their production and use |
| DE3508903A1 (en) | 1985-03-13 | 1986-09-18 | Hoechst Ag, 6230 Frankfurt | NEW 3-PYRIDYLMETHYLNAPHTYL DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS MEDICINAL PRODUCTS |
| EP0273647B1 (en) * | 1986-12-27 | 1992-03-11 | Takeda Chemical Industries, Ltd. | Coumaran derivatives, their production and use |
| FR2617478B1 (en) * | 1987-07-01 | 1990-01-05 | Esteve Labor Dr | NOVEL ARYL-HETEROARYL CETONES DERIVATIVES, THEIR PREPARATION PROCESS AND THEIR APPLICATION AS MEDICAMENTS |
| WO1992016527A1 (en) | 1991-03-22 | 1992-10-01 | Nippon Soda Co., Ltd. | 2-substituted pyridine derivative, production thereof, and agrohorticultural bactericide |
| ZA944647B (en) * | 1993-07-06 | 1995-01-06 | Astra Ab | Novel (1-phenyl-1-heterocyclyl)methanol and (1-phenyl-1-heterocyclcl)methylamine derivatives |
| SE9302333D0 (en) * | 1993-07-06 | 1993-07-06 | Ab Astra | NEW COMPOUNDS |
| EP0721943A4 (en) * | 1993-09-30 | 1996-09-04 | Yamanouchi Pharma Co Ltd | AZOL DERIVATIVES AND PHARMACEUTICAL PREPARATIONS |
| PL322028A1 (en) * | 1995-03-01 | 1998-01-05 | Yamanouchi Pharma Co Ltd | Derivatives of imidazoles and pharmaceutic composition containing them |
| AU710875B2 (en) | 1995-12-06 | 1999-09-30 | Tokuyama Corporation | Chromene compounds and photochromic materials |
| WO2000078727A1 (en) * | 1999-06-22 | 2000-12-28 | Takeda Chemical Industries, Ltd. | Process for the preparation of imidazole derivatives |
| EP1393262A1 (en) * | 1999-07-06 | 2004-03-03 | Bza Ag | Device for the utilisation of services |
| DE60026725T2 (en) | 1999-10-22 | 2006-09-07 | Takeda Pharmaceutical Co. Ltd. | METHOD FOR THE PRODUCTION OF OPTICALLY ACTIVE NAPHTHALINE DERIVATIVES AND OPTICAL RESOLVERS THEREOF |
-
1999
- 1999-04-22 CA CA002328973A patent/CA2328973A1/en not_active Abandoned
- 1999-04-22 AT AT99917102T patent/ATE293102T1/en not_active IP Right Cessation
- 1999-04-22 EP EP99917102A patent/EP1073640B1/en not_active Expired - Lifetime
- 1999-04-22 US US09/673,591 patent/US6573289B1/en not_active Expired - Lifetime
- 1999-04-22 AU AU35346/99A patent/AU3534699A/en not_active Abandoned
- 1999-04-22 WO PCT/JP1999/002143 patent/WO1999054309A1/en not_active Ceased
- 1999-04-22 DE DE69924717T patent/DE69924717T2/en not_active Expired - Lifetime
-
2003
- 2003-05-22 US US10/443,379 patent/US7084149B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20030236274A1 (en) | 2003-12-25 |
| CA2328973A1 (en) | 1999-10-28 |
| AU3534699A (en) | 1999-11-08 |
| WO1999054309A1 (en) | 1999-10-28 |
| DE69924717T2 (en) | 2006-03-09 |
| EP1073640B1 (en) | 2005-04-13 |
| US7084149B2 (en) | 2006-08-01 |
| EP1073640A1 (en) | 2001-02-07 |
| DE69924717D1 (en) | 2005-05-19 |
| US6573289B1 (en) | 2003-06-03 |
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